Lymphoma
is a group of blood and that develop from . The name typically refers to just the cancerous versions rather than all such tumors. Signs and symptoms may include enlarged lymph nodes, fever, drenching sweats, unintended weight loss, itching, and constantly feeling tired. The enlarged lymph nodes are usually painless. The sweats are most common at night.
Underlined words are explained — tap any of them.
Symptoms — what it feels like
- ·Enlarged nodes, fever, sweats, unintended weight loss, itching, feeling tired
How it's found
- · node
Treatment
- ·, therapy, proton therapy, targeted therapy,
Outlook
- ·Average five year survival 85% (USA)
The sections below are general education drawn from public guidelines (NHS, Mayo, CPIC, WHO, ICMR). They are not individually reviewed by a clinician and are not medical advice — always talk to a doctor about your own health.
Genes that change how certain drugs work — and that differ in South Asians. This is education, not a dosing tool; genotype-guided prescribing is a clinician decision.
Some people are born with red blood cells that can't handle certain 'stressful' medicines. Give those drugs and the red cells burst, causing sudden . A simple blood test tells the doctor whether a drug like an anti-malaria pill is safe for that person.
South Asian signal: G6PD deficiency is common across India: an all-India systematic review found an overall ~1.9% prevalence (range 0.8-6.3%), but tribal/vulnerable groups run far higher - ~7.7% overall in tribal communities and up to ~27% in some groups. The G6PD Mediterranean (563C>T) variant, a severe (Class II) variant, is the commonest deficient allele in India (~60% of deficient cases), so many Indian deficients are the high-risk severe type.
Prescriber note: Screen for G6PD status before prescribing primaquine/tafenoquine (radical cure of vivax malaria), dapsone, or rasburicase; rasburicase is contraindicated in G6PD deficiency. Because the severe Mediterranean variant predominates in India, do not assume mild African-type deficiency. CPIC advises that in G6PD-deficient individuals, drugs with haemolytic potential (e.g. rasburicase - formally contraindicated; primaquine, dapsone, and other listed oxidants) should be avoided or used only with explicit risk-benefit justification and monitoring, and that higher-risk ancestries be screened before such drugs.
Not a dosing tool. Genotype-guided prescribing is a clinician decision; genotyping access in India is limited.